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rs1085307975

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome4
Position70637844
GeneENAM
is asnp
is mentioned by
dbSNPrs1085307975
dbSNP (old)rs1085307975
ClinGenrs1085307975
ebirs1085307975
HLIrs1085307975
Exacrs1085307975
Gnomadrs1085307975
Varsomers1085307975
Maprs1085307975
PheGenIrs1085307975
Biobankrs1085307975
1000 genomesrs1085307975
hgdprs1085307975
ensemblrs1085307975
gopubmedrs1085307975
geneviewrs1085307975
scholarrs1085307975
googlers1085307975
pharmgkbrs1085307975
gwascentralrs1085307975
openSNPrs1085307975
23andMers1085307975
23andMe allrs1085307975
SNPshotrs1085307975
SNPdbers1085307975
MSV3drs1085307975
GWAS Ctlgrs1085307975
Max Magnitude0
ClinVar
Risk rs1085307975(G;G)
Alt rs1085307975(G;G)
Reference Rs1085307975(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ENAM
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.71503561dup
CLNSRC
CLNACC RCV000490006.1,